Novel esterases and uses thereof

ABSTRACT

The present invention relates to novel esterase, more particularly to esterase variants having improved activity compared to the esterase of SECS ID NO: 1 and the uses thereof for degrading polyester containing material, such as plastic products. The esterases of the invention are particularly suited to degrade polyethylene terephthalate, and material containing polyethylene terephthalate.

The present invention relates to novel esterases, more particularly toesterases having improved activity compared to a parent esterase and theuses thereof for degrading polyester containing material, such asplastic products. The esterases of the invention are particularly suitedto degrade polyethylene terephthalate, and material containingpolyethylene terephthalate.

BACKGROUND

Esterases are able to catalyze the hydrolysis of a variety of polymers,including polyesters. In this context, esterases have shown promisingeffects in a number of industrial applications, including as detergentsfor dishwashing and laundry applications, as degrading enzymes forprocessing biomass and food, as biocatalysts in detoxification ofenvironmental pollutants or for the treatment of polyester fabrics inthe textile industry. In the same way, the use of esterases as degradingenzymes for hydrolyzing polyethylene terephthalate (PET) is ofparticular interest. Indeed, PET is used in a large number of technicalfields, such as in the manufacture of clothes, carpets, or in the formof a thermoset resin for the manufacture of packaging or automobileplastics or other parts, and PET accumulation in landfills becomes anincreasing ecological problem.

Among esterases, cutinases, also known as cutin hydrolases (EC3.1.1.74), are of particular interest. Cutinases have been identifiedfrom various fungi (P. E. Kolattukudy in “Lipases”, Ed. B. Borg-strómand H. L. Brockman, Elsevier 1984, 471-504), bacteria and plant pollen.Recently, metagenomics approaches have led to identification ofadditional esterases.

The enzymatic degradation is considered as an interesting solution todecrease such plastic waste accumulation. Indeed, enzymes may acceleratehydrolysis of polyester containing material, and more particularly ofplastic products, even up to the monomer level. Furthermore, thehydrolysate (i.e., monomers and oligomers) can be recycled as materialfor synthesizing new polymers.

In this context, several esterases have been identified as candidatedegrading enzymes. For instance, several variants of the esterase ofFusarium solani pisi have been published (Appl. Environm. Microbiol. 64,2794-2799, 1998; Proteins: Structure, Function and Genetics26,442-458,1996).

However, there is still a need for esterases with improved activity toallow a process with higher efficiency and thereby to enhance thecompetitiveness of biological polyester degrading process.

SUMMARY OF THE INVENTION

The present invention provides new variants of esterase exhibitingincreased activity compared to a parent, or wild-type esterase. Theseesterases are particularly useful in processes for degrading plasticmaterial and product, such as plastic material and product containingPET. More particularly, the present invention provides variants of anesterase having the amino acid sequence as set forth in SEQ ID No 1,that corresponds to the amino acids 36 to 293 of the amino acid sequenceof the metagenome-derived cutinase described in Sulaiman et al., ApplEnviron Microbiol. 2012 Mar, or to the amino acids 36 to 293 of theamino acid sequence referenced G9BY57 in SwissProt.

In this regard, it is an object of the invention to provide an esterasevariant which (i) has at least 75%, 80%, 85%, 90%, 95% or 99% identityto the full length amino acid sequence set forth in SEQ ID No 1, and(ii) has at least one substitution at a position selected from F208,T157, T176, S65, G53, A121, V170, S223, P58, A62, A64, L67, A68, N85,T86, R89, D91, P93, R96, G128, M131, G133, G134, L152, T153, P154, H156,A178, P179, H183, S206, A209, P210 or N211, wherein the positions arenumbered by reference to the amino acid sequence set forth in SEQ ID No1, and (iii) exhibits increased polyester degrading activity compared toan esterase of SEQ ID No 1.

More particularly, the esterase comprises at least one substitution at aposition selected from F208, T157, T176, G53, A121, V170, S65, or N211.

According to a particular embodiment, the esterase comprises at leastone substitution or combination of substitutions selected from the groupconsisting of G53L, S65T, A121R/W, T157E/Q/N/G, V170I, T176H/N/Q,F208W/I/L/G/S/N/A/R/T, N211Q, F208W+V170I, Y92P+F208L, Y92P+F208W,T176H+F208W, V170I+A121S, V170I+A121S+S223A, F208W+T157Q, F208W+T157N,F208W+T157S, F208W+S65T, F208W+T157E, F208W+D203C+S248C,F2081+D203C+S248C as compared to SEQ ID No 1.

According to a particular embodiment, the esterase further comprises atleast one substitution, in addition to one or more of the above listedsubstitutions, at a position selected from G59, Y60, T61, D63, S66, F90,Y92, H129, G132, W155 and V177. Advantageously, the additionalsubstitution is selected from Y60M/F, T61M/V, D63N/Q, S66H, F90W, andY92G/N/P/Q/T.

In another particular embodiment, the esterase comprises at least onesubstitution selected from the group consisting of Y60M, T61M/V, D63N/Q,S66H, F90W, and Y92G/N/P/Q/T.

In another particular embodiment, the esterase variant comprises atleast two substitutions at positions selected from G53, P58, G59, Y60,T61, A62, D63, A64, S65, S66, L67, A68, N85, T86, R89, F90, D91, Y92,P93, R96, A121, G128, H129, M131, G132, G133, G134, L152, T153, P154,W155, H156, T157, V170, T176, V177, A178, H183, S206, F208, A209, P210,S223 and N211.

It is another object of the invention to provide a nucleic acid encodingan esterase of the invention. The present invention also relates to anexpression cassette or an expression vector comprising said nucleicacid, and to a host cell comprising said nucleic acid, expressioncassette or vector.

It is a further object of the invention to provide a method of producingan esterase of the invention comprising:

(a) culturing the host cell according to the invention under conditionssuitable to express a nucleic acid encoding an esterase; and optionally

(b) recovering said esterase from the cell culture.

The present invention also relates to a method of degrading a plasticproduct containing at least one polyester comprising

(a) contacting the plastic product with an esterase or host cellaccording to the invention, thereby degrading the plastic product; andoptionally

(b) recovering monomers and/or oligomers.

DETAILED DESCRIPTION OF THE INVENTION Definitions

The present disclosure will be best understood by reference to thefollowing definitions.

Herein, the terms “peptide”, “polypeptide”, “protein”, “enzyme” refer toa chain of amino acids linked by peptide bonds, regardless of the numberof amino acids forming said chain. The amino acids are hereinrepresented by their one-letter or three-letters code according to thefollowing nomenclature: A: alanine (Ala); C: cysteine (Cys); D: asparticacid (Asp); E: glutamic acid (Glu); F: phenylalanine (Phe); G: glycine(Gly); H: histidine (His); I: isoleucine (Ile); K: lysine (Lys); L:leucine (Leu); M: methionine (Met); N: asparagine (Asn); P: proline(Pro); Q: glutamine (Gln); R: arginine (Arg); S: serine (Ser); T:threonine (Thr); V: valine (Val); W: tryptophan (Trp) and Y: tyrosine(Tyr).

The term “esterase” refers to an enzyme which belongs to a class ofhydrolases classified as

EC 3.1.1 according to Enzyme Nomenclature that catalyzes the hydrolysisof esters into an acid and an alcohol. The term “cutinase” or “cutinhydrolase” refers to the esterases classified as EC 3.1.1.74 accordingto Enzyme Nomenclature that is able to catalyse the chemical reaction ofproduction of cutin monomers from cutin and water.

The terms “wild-type protein” or “parent protein” are usedinterchangeably and refer to the non-mutated version of a polypeptide asit appears naturally. In the present case, the parent esterase refers tothe esterase having the amino acid sequence as set forth in SEQ ID No 1.

Accordingly, the terms “mutant” and “variant” may be usedinterchangeably to refer to polypeptides derived from SEQ ID No 1 andcomprising a modification or an alteration, i.e., a substitution,insertion, and/or deletion, at one or more (e.g., several) positions andhaving a polyester degrading activity. The variants may be obtained byvarious techniques well known in the art. In particular, examples oftechniques for altering the DNA sequence encoding the wild-type protein,include, but are not limited to, site-directed mutagenesis, randommutagenesis and synthetic oligonucleotide construction.

The term “modification” or “alteration” as used herein in relation to aposition or amino acid means that the amino acid in the particularposition has been modified compared to the amino acid of the wild-typeprotein.

A “substitution” means that an amino acid residue is replaced by anotheramino acid residue. Preferably, the term “substitution” refers to thereplacement of an amino acid residue by another selected from thenaturally-occurring standard 20 amino acid residues, rare naturallyoccurring amino acid residues (e.g. hydroxyproline, hydroxylysine,allohydroxylysine, 6-N-methylysine, N-ethylglycine, N-methylglycine,N-ethylasparagine, allo-isoleucine, N-methylisoleucine, N-methylvaline,pyroglutamine, aminobutyric acid, ornithine, norleucine, norvaline), andnon-naturally occurring amino acid residue, often made synthetically,(e.g. cyclohexyl-alanine). Preferably, the term “substitution” refers tothe replacement of an amino acid residue by another selected from thenaturally-occurring standard 20 amino acid residues (G, P, A, V, L, I,M, C, F, Y, W, H, K, R, Q, N, E, D, S and T). The sign “+” indicates acombination of substitutions. In the present document, the followingterminology is used to designate a substitution: L82A denotes that aminoacid residue (Leucine, L) at position 82 of the parent sequence ischanged to an Alanine (A). A121V/I/M denotes that amino acid residue(Alanine, A) at position 121 of the parent sequence is substituted byone of the following amino acids: Valine (V), Isoleucine (I), orMethionine (M). The substitution can be a conservative ornon-conservative substitution. Examples of conservative substitutionsare within the groups of basic amino acids (arginine, lysine andhistidine), acidic amino acids (glutamic acid and aspartic acid), polaramino acids (glutamine, asparagine and threonine), hydrophobic aminoacids (methionine, leucine, isoleucine, cysteine and valine), aromaticamino acids (phenylalanine, tryptophan and tyrosine), and small aminoacids (glycine, alanine and serine).

The term “deletion”, used in relation to an amino acid, means that theamino acid has been removed or is absent.

The term “insertion” means that one or more amino acids have been added.

Unless otherwise specified, the positions disclosed in the presentapplication are numbered by reference to the amino acid sequence setforth in SEQ ID No 1.

As used herein, the term “sequence identity” or “identity” refers to thenumber (or fraction expressed as a percentage %) of matches (identicalamino acid residues) between two polypeptide sequences. The sequenceidentity is determined by comparing the sequences when aligned so as tomaximize overlap and identity while minimizing sequence gaps. Inparticular, sequence identity may be determined using any of a number ofmathematical global or local alignment algorithms, depending on thelength of the two sequences. Sequences of similar lengths are preferablyaligned using a global alignment algorithms (e.g. Needleman and Wunschalgorithm; Needleman and Wunsch, 1970) which aligns the sequencesoptimally over the entire length, while sequences of substantiallydifferent lengths are preferably aligned using a local alignmentalgorithm (e.g. Smith and Waterman algorithm (Smith and Waterman, 1981)or Altschul algorithm (Altschul et al., 1997; Altschul et al., 2005)).Alignment for purposes of determining percent amino acid sequenceidentity can be achieved in various ways that are within the skill inthe art, for instance, using publicly available computer softwareavailable on internet web sites such as http://blast.ncbi.nlm.nih.gov/or http://www.ebi.ac.uk/Tools/emboss/). Those skilled in the art candetermine appropriate parameters for measuring alignment, including anyalgorithms needed to achieve maximal alignment over the full length ofthe sequences being compared. For purposes herein, % amino acid sequenceidentity values refers to values generated using the pair wise sequencealignment program EMBOSS Needle that creates an optimal global alignmentof two sequences using the Needleman-Wunsch algorithm, wherein allsearch parameters are set to default values, i.e. Scoringmatrix=BLOSUM62, Gap open=10, Gap extend=0.5, End gap penalty=false, Endgap open=10 and End gap extend=0.5.

The “protein conformation” or “crystal structure” refers to the threedimensional structure of the protein.

The term “recombinant” refers to a nucleic acid construct, a vector, apolypeptide or a cell produced by genetic engineering.

The term “expression”, as used herein, refers to any step involved inthe production of a polypeptide including, but being not limited to,transcription, post-transcriptional modification, translation,post-translational modification, and secretion.

The term “expression cassette” denotes a nucleic acid constructcomprising a coding region, i.e. a nucleic acid of the invention, and aregulatory region, i.e. comprising one or more control sequences,operably linked.

As used herein, the term “expression vector” means a DNA or RNA moleculethat comprises an expression cassette of the invention. Preferably, theexpression vector is a linear or circular double stranded DNA molecule.

A “polymer” refers to a chemical compound or mixture of compounds whosestructure is constituted of multiple monomers (repeat units) linked bycovalent chemical bonds. Within the context of the invention, the termpolymer includes natural or synthetic polymers, constituted of a singletype of repeat unit (i.e., homopolymers) or of a mixture of differentrepeat units (i.e., copolymers or heteropolymers). According to theinvention, “oligomers” refer to molecules containing from 2 to about 20monomers.

In the context of the invention, a “polyester containing material” or“polyester containing product” refers to a product, such as plasticproduct, comprising at least one polyester in crystalline,semi-crystalline or totally amorphous forms. In a particular embodiment,the polyester containing material refers to any item made from at leastone plastic material, such as plastic sheet, tube, rod, profile, shape,film, massive block etc., which contains at least one polyester, andpossibly other substances or additives, such as plasticizers, mineral ororganic fillers. In another particular embodiment, the polyestercontaining material refers to a plastic compound, or plasticformulation, in a molten or solid state, suitable for making a plasticproduct.

In the present description, “polyesters” encompass but is not limited topolyethylene terephthalate (PET), polytrimethylene terephthalate (PTT),polybutylene terephthalate (PBT), polyethylene isosorbide terephthalate(PEIT), polylactic acid (PLA), polyhydroxyalkanoate (PHA), polybutylenesuccinate (PBS), polybutylene succinate adipate (PBSA), polybutyleneadipate terephthalate (PBAT), polyethylene furanoate (PEF),polycaprolactone (PCL), poly(ethylene adipate) (PEA), polyethylenenaphthalate (PEN) and blends/mixtures of these polymers.

Novel Esterases with Improved Activity

The present invention provides novel esterases with improved activity.More particularly, the inventors have designed novel enzymes havingsuperior properties for use in industrial processes. With the aim toimprove the activity of esterases in conditions where industrialdegradation of plastic products can be performed, the inventors havedeveloped novel esterases derived from the esterase of SEQ ID No 1 thatshow higher activity compared to this parent esterase. The esterases ofthe invention are particularly suited to degrade plastic productcontaining PET. The esterases of the invention exhibit an increasedspecific activity and/or an increased ability to adsorb on a polymer,compared to the esterase of SEQ ID No 1. Interestingly, the inventorshave identified specific amino acid residues, which are intended to bein contact with a polymer substrate in the crystal structure of theprotein that may be advantageously modified to promote the contact ofthe substrate with the protein and thereby increasing the adsorption ofthe polymer and/or the activity of the protein on this polymer.

It is thus an object of the present invention to provide an esterasewhich (i) has at least 75%, 80%, 85%, 90%, 95% or 99% identity to thefull length amino acid sequence set forth in SEQ ID No 1, (ii) containsat least one amino acid modification as compared to SEQ ID NO: 1, and(iii) exhibits increased polyester degrading activity as compared to theesterase of SEQ ID No 1.

Within the context of the invention, the term “increased activity” or“increased degrading activity” indicates an increased ability of theenzyme to degrade a plastic product or material, and more particularly apolyester containing plastic product or material, as compared to theesterase of SEQ ID No 1. Such an increase is typically of about 1-fold,2-fold, 3-fold, 4-fold, 5-fold, or more. Particularly, the esterasevariant has a polyester degrading activity at least 10% greater than thepolyester degrading activity of the esterase of SEQ ID No 1, preferablyat least 20%, 50%, 100%, 200%, 300%, or more greater.

The activity of a protein may be evaluated by the one skilled in theart, according to methods known per se in the art. For instance, theactivity can be assessed by the measurement of the specific esteraseactivity rate, the measurement of the specific polyester'sdepolymerization activity rate, the measurement of the rate to degrade asolid polyester compound dispersed in an agar plate, or the measurementof the specific polyester's depolymerization activity rate in reactor.

Within the context of the invention, the terms “specific activity” or“specific degrading activity” designate the initial rate of oligomersand/or monomers released under suitable conditions of temperature, pHand buffer, when contacting the polyester containing plastic productwith a degrading enzyme, such as an esterase according to the invention.As an example, the specific activity of PET hydrolysis corresponds toμmol of PET hydrolysed/min or mg of equivalent TA produced/hour and permg of enzyme as determined in the linear part of the hydrolysis curve.

The ability of a protein to adsorb on a substrate may be evaluated bythe one skilled in the art, according to methods known per se in theart. For instance, the proteic content or the residual esteraseactivity, residual polyester's depolymerization activity, residualdegradation of a solid polyester compound dispersed in an agar plate, orresidual polyester's depolymerization activity in reactor can bemeasured from a solution containing the esterase of the invention andwherein the esterase has been previously incubated with a substrateunder suitable conditions where no enzymatic reaction can occur.

In a particular embodiment, the variants of the invention have both animproved thermostability and an increased polyester degrading activityas compared to the esterase of SEQ ID No 1.

Within the context of the invention, the term “increasedthermostability” indicates an increased ability of the enzyme to resistto changes in its chemical and/or physical structure at hightemperatures, and more particularly at temperature between 50° C. and90° C., as compared to the esterase of SEQ ID No 1. Such an increase istypically of about 1-fold, 2-fold, 3-fold, 4-fold, 5-fold, or more.Particularly, the esterases of the present invention may exhibit anincreased melting temperature (Tm) as compared to the esterase of SEQ IDNo 1. In the context of the present invention, the melting temperaturerefers to the temperature at which half of the protein/enzyme populationconsidered is unfolded or misfolded. Typically, the esterase of theinvention shows an increased Tm of about 1° C., 2° C., 3° C., 4° C., 5°C., 10° C. or more, as compared to the Tm of the esterase of SEQ ID No1.

In particular, the esterases of the present invention can have anincreased half-life at a temperature between 50° C. and 90° C., ascompared to the esterase of SEQ ID No 1. Furthermore, at suchtemperature, the esterases of the invention may exhibit greaterdegrading activity as compared to the esterase of SEQ ID No 1.

The thermostability of a protein may be evaluated by the one skilled inthe art, according to methods known per se in the art. For instance,thermostability can be assessed by analysis of the protein folding usingcircular dichroism. Alternatively or in addition, thermostability can beassessed by measuring the residual esterase activity and/or the residualpolyester depolymerization activity of the enzyme after incubation atdifferent temperatures. The ability to perform multiple rounds ofpolyester's depolymerization assays at different temperatures can alsobe evaluated. A rapid and valuable test may consist on the evaluation,by halo diameter measurement, of the enzyme ability to degrade a solidpolyester compound dispersed in an agar plate after incubation atdifferent temperatures. Preferably, a Differential Scanning Fluorimetry(DSF) is performed to assess the thermostability of a protein/enzyme.More particularly, the DSF may be used to quantify the change in thermaldenaturation temperature of a protein and thereby to determine itsmelting temperature (Tm). In the context of the invention, and unlessspecific indications, the Tm is measured using DSF as exposed in theexperimental part. In the context of the invention, comparisons of Tmare performed with Tm that are measured under same conditions (e.g. pH,nature and amount of polyesters, etc.).

The esterases of the invention may comprise one or several modificationsas disclosed below.

According to the invention, the esterase is a variant of the esterase ofSEQ ID No 1, which has at least 75%, 80%, 85%, 90%, 95% or 99% identityto the full length amino acid sequence set forth in SEQ ID No 1, andwhich has at least one substitution at a position selected from G53,P58, A62, A64, S65, L67, A68, N85, T86, R89, D91, P93, R96, A121, G128,M131, G133, G134, L152, T153, P154, H156, T157, V170, T176, A178, P179,H183, S206, F208, A209, P210, N211, or S223 wherein the positions arenumbered by reference to the amino acid sequence set forth in SEQ ID No1.

According to the invention, the targeted amino acid(s) may be replacedby any one of the 19 other amino acids.

Preferably, the esterase variant comprises a least one substitution at aposition selected from G53, A62, A64, S65, A68, N85, T86, R89, A121,T157, V170, T176, S206, F208, N211, S223.

More preferably, the esterase variant comprises at least onesubstitution at a position selected from G53, S65, A121, T157, V170,T176, F208 or N211.

In a particular embodiment, the esterase variant comprises a least onesubstitution selected from G53L, S65T, A121R/W, T157E/Q/N/G, V170I,T176H/N/Q, F208W/I/L/G/S/N/A/R/T and N211Q. Preferably, the esterasevariant comprises at least one substitution selected from F208W/I/L. Ina preferred embodiment, the esterase variant comprises a least thesubstitution F208W. In another preferred embodiment, the esterasevariant comprises at least the substitution F208I.

In a particular embodiment, the esterase variant further comprises, inaddition to at least one substitution described above, at least oneadditional substitution at a position selected from G59, Y60, T61, D63,S66, F90, Y92, H129, G132, W155 and V177. Preferably, the one or moreadditional substitutions are selected from Y60M/F, T61M/V, D63N/Q, S66H,F9OW, and Y92G/N/P/Q/T.

Alternatively or in addition, at least one of the additionalsubstitution is selected from A121S, T157S or S223A.

In another particular embodiment, the esterase variant comprises atleast one substitution, and in particular a single substitution, ascompared to SEQ ID No 1 at positions selected from Y60, G53, T61, A62,D63, S65, S66, F90, Y92, A121, H129, T157, T176, V170, V177, F208, N211,and wherein the substitutions are different from Y60A/F, T61A/G, A62G/S,D63T/R, S66A, F90A/R/Y, Y92A, H129W and V177A. Preferably, the esterasecomprises one or more substitutions selected from the group consistingof Y60M, T61M/V, D63N/Q, S66H, F9OW, and Y92G/N/P/Q/T. In anotherparticular embodiment, the esterase comprises a single substitutionselected from the group consisting of Y60M, T61M/V, D63N/Q, S66H, F90W,and Y92G/N/P/Q/T.

According to a particular embodiment, the variant comprises at least onesubstitution selected from D63N/Q.

According to a particular embodiment, the variant comprises at least onesubstitution selected from Y92G/N/P/Q/T, preferably Y92P.

In another particular embodiment, the esterase variant comprises atleast one substitution at a position selected from D63, A64, A68, N85,R89, W155, T176, S206, F208 or N211.

In another particular embodiment, the esterase variant comprises atleast two substitutions at positions selected from G53, P58, G59, Y60,T61, A62, D63, A64, S65, S66, L67, A68, N85, T86, R89, F90, D91, Y92,P93, R96, A121, G128, H129, M131, G132, G133, G134, L152, T153, P154,W155, H156, T157, V170, T176, V177, A178, H183, S206, F208, A209, P210,S223 and N211.

In another particular embodiment, the esterase variant comprises atleast two substitutions at positions selected from G53, Y60, T61, D63,S65, S66, F90, Y92, A121, T157, V170, T176, V177, F208, S223 and N211.

Particularly, the esterase variant comprises at least two substitutionsat positions selected from S65, Y92, A121, T157, V170, T176, F208 andS223.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+V170I.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of Y92P+F208L.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of Y92P+F208W.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of T176H+F208W.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of V170I+A121S.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of V170I+A121S+S223A.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+T157Q.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+T157N.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+T157S.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+S65T.

According to a particular embodiment, the variant comprises at least thecombination of substitutions consisting of F208W+T157E.

In a particular embodiment, the esterase variant of the inventioncomprises one or several modifications and/or mutations as listed above.

Novel Esterases with Improved Activity and Thermostability

It is a further object of the invention to provide novel esterases thatexhibit both increased polyester degrading activity and increasedthermostability as compared to the esterase of SEQ ID No 1.

It is another object of the invention to provide an esterase which (i)has at least 75%, 80%, 85%, 90%, 95% or 99% identity to the full lengthamino acid sequence set forth in SEQ ID No 1, (ii) contains at least oneamino acid modification as compared to SEQ ID NO: 1, and (iii) exhibitsboth an increased thermostability and an increased activity as comparedto the esterase of SEQ ID No 1.

Advantageously, the variant comprises at least one substitution selectedfrom T61M, Y92G/P, F208W, Y92P+F208W, and F208W+V170I and exhibits bothan increased thermostability and an increased activity as compared tothe esterase of SEQ ID No 1.

Advantageously, the esterase variant comprises at least one mutation asdisclosed above and at least one additional substitution at a positionselected from D203C+S248C by reference to SEQ ID No 1. Advantageously,the variant comprises at least the substitution(s) selected fromF208W+D203C+S248C or F2081+D203C+S248C and exhibits both an increasedthermostability and an increased activity as compared to the esterase ofSEQ ID No 1.

Polyester Degrading Activity of the Variant

It is an object of the invention to provide new enzymes having anesterase activity. In a particular embodiment, the enzyme of theinvention further exhibits a cutinase activity.

In a particular embodiment, the esterase of the invention has apolyester degrading activity, preferably a polyethylene terephthalatedegrading activity.

In another particular embodiment, the esterase of the invention also hasa PBAT degrading activity.

Advantageously, the esterase variant of the invention exhibits apolyester degrading activity at least in a range of temperatures from20° C. to 90° C., preferably from 40° C. to 80° C., more preferably from50° C. to 70° C., even more preferably from 60° C. to 70° C., even morepreferably at 65° C. In a particular embodiment, the esterase variant ofthe invention exhibits a polyester degrading activity at 70° C. In aparticular embodiment, the polyester degrading activity is stillmeasurable at a temperature between 60° C. and 90° C.

In a particular embodiment, the esterase variant of the invention has anincreased polyester degrading activity at a given temperature, comparedto the esterase of SEQ ID No 1, and more particularly at a temperaturebetween 40° C. and 80° C., more preferably between 50° C. and 70° C.,even more preferably between 60° C. and 70° C., even more preferably at65° C. In a particular embodiment, the esterase variant has a polyesterdegrading activity at 65° C. at least 5% higher than the polyesterdegrading activity of the esterase of SEQ ID No 1, preferably at least10%, 20%, 50%, 100%, 200%, 300%, or more higher. In a particularembodiment, the esterase variant has a polyester degrading activity at65° C. at least 10% greater than the polyester degrading activity of theesterase of SEQ ID No 1, preferably at least 20%, 50%, 100%, 200%, 300%,or more greater.

In a particular embodiment, the esterase variant of the inventionexhibits a measurable esterase activity at least in a range of pH from 5to 11, preferably in a range of pH from 6 to 9, more preferably in arange of pH from 6.5 to 9, even more preferably in a range of pH from6.5 to 8.

Nucleic Acids, Expression Cassette, Vector, Host Cell

It is a further object of the invention to provide a nucleic acidencoding an esterase as defined above.

As used herein, the term “nucleic acid”, “nucleic sequence,”“polynucleotide”, “oligonucleotide” and “nucleotide sequence” are usedinterchangeably and refer to a sequence of deoxyribonucleotides and/orribonucleotides. The nucleic acids can be DNA (cDNA or gDNA), RNA, or amixture of the two. It can be in single stranded form or in duplex formor a mixture of the two. It can be of recombinant, artificial and/orsynthetic origin and it can comprise modified nucleotides, comprisingfor example a modified bond, a modified purine or pyrimidine base, or amodified sugar. The nucleic acids of the invention can be in isolated orpurified form, and made, isolated and/or manipulated by techniques knownper se in the art, e.g., cloning and expression of cDNA libraries,amplification, enzymatic synthesis or recombinant technology. Thenucleic acids can also be synthesized in vitro by well-known chemicalsynthesis techniques, as described in, e.g., Belousov (1997) NucleicAcids Res. 25:3440-3444.

The invention also encompasses nucleic acids which hybridize, understringent conditions, to a nucleic acid encoding an esterase as definedabove. Preferably, such stringent conditions include incubations ofhybridization filters at about 42° C. for about 2.5 hours in 2×SSC/0.1%SDS, followed by washing of the filters four times of 15 minutes in1×SSC/0.1% SDS at 65° C. Protocols used are described in such referenceas Sambrook et al. (Molecular Cloning: a Laboratory Manual, Cold SpringHarbor Press, Cold Spring Harbor N.Y. (1988)) and Ausubel (CurrentProtocols in Molecular Biology (1989)).

The invention also encompasses nucleic acids encoding an esterase of theinvention, wherein the sequence of said nucleic acids, or a portion ofsaid sequence at least, has been engineered using optimized codon usage.

Alternatively, the nucleic acids according to the invention may bededuced from the sequence of the esterase according to the invention andcodon usage may be adapted according to the host cell in which thenucleic acids shall be transcribed. These steps may be carried outaccording to methods well known to one skilled in the art and some ofwhich are described in the reference manual Sambrook et al. (Sambrook etal., 2001).

Nucleic acids of the invention may further comprise additionalnucleotide sequences, such as regulatory regions, i.e., promoters,enhancers, silencers, terminators, signal peptides and the like that canbe used to cause or regulate expression of the polypeptide in a selectedhost cell or system.

The present invention further relates to an expression cassettecomprising a nucleic acid according to the invention operably linked toone or more control sequences that direct the expression of said nucleicacid in a suitable host cell. Typically, the expression cassettecomprises, or consists of, a nucleic acid according to the inventionoperably linked to a control sequence such as transcriptional promoterand/or transcription terminator. The control sequence may include apromoter that is recognized by a host cell or an in vitro expressionsystem for expression of a nucleic acid encoding an esterase of thepresent invention. The promoter contains transcriptional controlsequences that mediate the expression of the enzyme. The promoter may beany polynucleotide that shows transcriptional activity in the host cellincluding mutant, truncated, and hybrid promoters, and may be obtainedfrom genes encoding extracellular or intracellular polypeptides eitherhomologous or heterologous to the host cell. The control sequence mayalso be a transcription terminator, which is recognized by a host cellto terminate transcription. The terminator is operably linked to the3′-terminus of the nucleic acid encoding the esterase. Any terminatorthat is functional in the host cell may be used in the presentinvention. Typically, the expression cassette comprises, or consists of,a nucleic acid according to the invention operably linked to atranscriptional promoter and a transcription terminator.

The invention also relates to a vector comprising a nucleic acid or anexpression cassette as defined above.

The term “vector” refers to DNA molecule used as a vehicle to transferrecombinant genetic material into a host cell. The major types ofvectors are plasmids, bacteriophages, viruses, cosmids, and artificialchromosomes. The vector itself is generally a DNA sequence that consistsof an insert (a heterologous nucleic acid sequence, transgene) and alarger sequence that serves as the “backbone” of the vector. The purposeof a vector which transfers genetic information to the host is typicallyto isolate, multiply, or express the insert in the target cell. Vectorscalled expression vectors (expression constructs) are specificallyadapted for the expression of the heterologous sequences in the targetcell, and generally have a promoter sequence that drives expression ofthe heterologous sequences encoding a polypeptide. Generally, theregulatory elements that are present in an expression vector include atranscriptional promoter, a ribosome binding site, a terminator, andoptionally present operator. Preferably, an expression vector alsocontains an origin of replication for autonomous replication in a hostcell, a selectable marker, a limited number of useful restriction enzymesites, and a potential for high copy number. Examples of expressionvectors are cloning vectors, modified cloning vectors, specificallydesigned plasmids and viruses. Expression vectors providing suitablelevels of polypeptide expression in different hosts are well known inthe art. The choice of the vector will typically depend on thecompatibility of the vector with the host cell into which the vector isto be introduced.

It is another object of the invention to provide a host cell comprisinga nucleic acid, an expression cassette or a vector as described above.The present invention thus relates to the use of a nucleic acid,expression cassette or vector according to the invention to transform,transfect or transduce a host cell. The choice of the vector willtypically depend on the compatibility of the vector with the host cellinto which it must be introduced.

According to the invention, the host cell may be transformed,transfected or transduced in a transient or stable manner. Theexpression cassette or vector of the invention is introduced into a hostcell so that the cassette or vector is maintained as a chromosomalintegrant or as a self-replicating extra-chromosomal vector. The term“host cell” also encompasses any progeny of a parent host cell that isnot identical to the parent host cell due to mutations that occur duringreplication. The host cell may be any cell useful in the production of avariant of the present invention, e.g., a prokaryote or a eukaryote. Theprokaryotic host cell may be any Gram-positive or Gram-negativebacterium. The host cell may also be an eukaryotic cell, such as ayeast, fungal, mammalian, insect or plant cell. In a particularembodiment, the host cell is selected from the group of Escherichiacoli, Bacillus, Streptomyces, Trichoderma, Aspergillus, Saccharomyces,Pichia or Yarrowia.

The nucleic acid, expression cassette or expression vector according tothe invention may be introduced into the host cell by any method knownby the skilled person, such as electroporation, conjugation,transduction, competent cell transformation, protoplast transformation,protoplast fusion, biolistic “gene gun” transformation, PEG-mediatedtransformation, lipid-assisted transformation or transfection,chemically mediated transfection, lithium acetate-mediatedtransformation, liposome-mediated transformation.

Optionally, more than one copy of a nucleic acid, cassette or vector ofthe present invention may be inserted into a host cell to increaseproduction of the variant.

In a particular embodiment, the host cell is a recombinantmicroorganism. The invention indeed allows the engineering ofmicroorganisms with improved capacity to degrade polyester containingmaterial. For instance, the sequence of the invention may be used tocomplement a wild type strain of a fungus or bacterium already known asable to degrade polyester, in order to improve and/or increase thestrain capacity.

Production of Esterase Variant

It is another object of the invention to provide a method of producingthe esterase variant of the invention, comprising expressing a nucleicacid encoding the esterase and optionally recovering the esterase.

In particular, the present invention relates to in vitro methods ofproducing an esterase of the present invention comprising (a) contactinga nucleic acid, cassette or vector of the invention with an in vitroexpression system; and (b) recovering the esterase produced. In vitroexpression systems are well-known by the person skilled in the art andare commercially available.

Preferably, the method of production comprises

(a) culturing a host cell that comprises a nucleic acid encoding anesterase of the invention under conditions suitable to express thenucleic acid; and optionally

(b) recovering said esterase from the cell culture.

Advantageously, the host cell is a recombinant Bacillus, recombinant E.coli, recombinant Aspergillus, recombinant Trichoderma, recombinantStreptomyces, recombinant Saccharomyces, recombinant Pichia orrecombinant Yarrowia lipolytica.

The host cells are cultivated in a nutrient medium suitable forproduction of polypeptides, using methods known in the art. For example,the cell may be cultivated by shake flask cultivation, or small-scale orlarge-scale fermentation (including continuous, batch, fed-batch, orsolid state fermentations) in laboratory or industrial fermentorsperformed in a suitable medium and under conditions allowing the enzymeto be expressed and/or isolated. The cultivation takes place in asuitable nutrient medium, from commercial suppliers or preparedaccording to published compositions (e.g., in catalogues of the AmericanType Culture Collection).

If the esterase is excreted into the nutrient medium, the esterase canbe recovered directly from the culture supernatant. Conversely, theesterase can be recovered from cell lysates or after permeabilisation.The esterase may be recovered using any method known in the art. Forexample, the esterase may be recovered from the nutrient medium byconventional procedures including, but not limited to, collection,centrifugation, filtration, extraction, spray-drying, evaporation, orprecipitation. Optionally, the esterase may be partially or totallypurified by a variety of procedures known in the art including, but notlimited to, chromatography (e.g., ion exchange, affinity, hydrophobic,chromatofocusing, and size exclusion), electrophoretic procedures (e.g.,preparative isoelectric focusing), differential solubility (e.g.,ammonium sulfate precipitation), SDS-PAGE, or extraction to obtainsubstantially pure polypeptides.

The esterase may be used as such, in purified form, either alone or incombinations with additional enzymes, to catalyze enzymatic reactionsinvolved in the degradation and/or recycling of a polyester containingmaterial, such as plastic products containing polyester. The esterasemay be in soluble form, or on solid phase. In particular, it may bebound to cell membranes or lipid vesicles, or to synthetic supports suchas glass, plastic, polymers, filter, membranes, e.g., in the form ofbeads, columns, plates and the like.

Composition

It is a further object of the invention to provide a compositioncomprising an esterase or a host cell of the invention. In the contextof the invention, the term “composition” encompasses any kind ofcompositions comprising an esterase of the invention. In a particularembodiment, the esterase is in isolated or at least partially purifiedform.

The composition may be liquid or dry, for instance in the form of apowder. In some embodiments, the composition is a lyophilisate. Forinstance, the composition may comprise the esterase and/or recombinantcells encoding the esterase of the invention or extract thereof, andoptionally excipients and/or reagents etc. Appropriate excipientsencompass buffers commonly used in biochemistry, agents for adjustingpH, preservatives such as sodium benzoate, sodium sorbate or sodiumascorbate, conservatives, protective or stabilizing agents such asstarch, dextrin, arabic gum, salts, sugars e.g. sorbitol, trehalose orlactose, glycerol, polyethyleneglycol, polyethene glycol, polypropyleneglycol, propylene glycol, sequestering agent such as EDTA, reducingagents, amino acids, a carrier such as a solvent or an aqueous solution,and the like. The composition of the invention may be obtained by mixingthe esterase with one or several excipients.

The composition of the invention may comprise from 0.1% to 99.9%,preferably from 0.1% to 50%, more preferably from 0.1% to 30%, even morepreferably from 0.1% to 5% by weight of the esterase of the inventionand from 0.1% to 99.9%, preferably from 50% to 99.9%, more preferablyfrom 70% to 99.9%, even more preferably from 95% to 99.9% by weight ofexcipient(s). A preferred composition comprises between 0.1 and 5% byweight of the esterase of the invention.

In a particular embodiment, the composition may further compriseadditional polypeptide(s) exhibiting an enzymatic activity. The amountsof esterase of the invention will be easily adapted by those skilled inthe art depending e.g., on the nature of the polyester containingmaterial to degrade and/or the additional enzymes/polypeptides containedin the composition.

In a particular embodiment, the esterase of the invention is solubilizedin an aqueous medium together with one or several excipients, especiallyexcipients which are able to stabilize or protect the polypeptide fromdegradation. For instance, the esterase of the invention may besolubilized in water, eventually with additional components, such asglycerol, sorbitol, dextrin, starch, glycol such as propanediol, salt,etc. The resulting mixture may then be dried so as to obtain a powder.Methods for drying such mixture are well known to the one skilled in theart and include, without limitation, lyophilisation, freeze-drying,spray-drying, supercritical drying, down-draught evaporation, thin-layerevaporation, centrifugal evaporation, conveyer drying, fluidized beddrying, drum drying or any combination thereof.

In a further particular embodiment, the composition of the inventioncomprises at least one recombinant cell expressing an esterase of theinvention, or an extract thereof. An “extract of a cell” designates anyfraction obtained from a cell, such as cell supernatant, cell debris,cell walls, DNA extract, enzymes or enzyme preparation or anypreparation derived from cells by chemical, physical and/or enzymatictreatment, which is essentially free of living cells.

Preferred extracts are enzymatically-active extracts. The composition ofthe invention may comprise one or several recombinant cells of theinvention or extract thereof, and optionally one or several additionalcells.

In a particular embodiment, the composition consists or comprises alyophilized culture medium of a recombinant microorganism expressing andexcreting an esterase of the invention. In a particular embodiment, thepowder comprises the esterase of the invention and astabilizing/solubilizing amount of glycerol, sorbitol or dextrin, suchas maltodextrine and/or cyclodextrine, starch, glycol such aspropanediol, and/or salt.

Use of the Esterase of the Invention

It is a further object of the invention to provide methods using anesterase of the invention for degrading in aerobic or anaerobicconditions and/or recycling polyester containing material, as plasticproducts made of or containing polyesters. The variant esterases of theinvention are particularly useful for degrading a plastic productcomprising PET.

It is therefore an object of the invention to use an esterase of theinvention, or corresponding recombinant cell or extract thereof, orcomposition for the enzymatic degradation of a polyester containingmaterial, such as a PET containing material.

It is another object of the invention to provide a method for degradinga plastic product containing at least one polyester, wherein the plasticproduct is contacted with an esterase or host cell or composition of theinvention, thereby degrading the plastic product. Advantageously,polyester(s) of the polyester containing material is (are) depolymerizedup to monomers and/or oligomers.

In an embodiment of the method of degradation, at least one polyester isdegraded to yield repolymerizable monomers and/or oligomers, which areadvantageously retrieved in order to be reused.

In an embodiment, polyester(s) of the polyester containing material is(are) fully degraded.

In a particular embodiment, the plastic product comprises at least onepolyester selected from polyethylene terephthalate (PET),polytrimethylene terephthalate (PTT), polybutylen terephthalate (PBT),polyethylene isosorbide terephthalate (PEIT), polylactic acid (PLA),polyhydroxyalkanoate (PHA), polybutylene succinate (PBS), polybutylenesuccinate adipate (PBSA), polybutylene adipate terephthalate (PBAT),polyethylene furanoate (PEF), polycaprolactone (PCL), poly(ethyleneadipate) (PEA), polyethylene naphthalate (PEN) and blends/mixtures ofthese materials, preferably polyethylene terephthalate. In a preferredembodiment, the polyester containing material comprises PET, and atleast monomers such as monoethylene glycol or terephthalic acid, and/oroligomers such as methyl-2-hydroxyethyl terephthalate (MHET),bis(2-hydroxyethyl) terephthalate (BHET), 2-hydroxyethyl benzoate (HEB)and dimethyl terephthalate (DMT) are recovered for recycling ormethanisation for instance.

The invention also relates to a method of producing monomers and/oroligomers from a polyester containing material, comprising exposing apolyester containing material to an esterase of the invention, orcorresponding recombinant cell or extract thereof, or composition, andoptionally recovering monomers and/or oligomers. The method of theinvention is particularly useful for producing monomers selected frommonoethylene glycol and terephthalic acid, and/or oligomers selectedfrom methyl-2-hydroxyethyl terephthalate (MHET), bis(2-hydroxyethyl)terephthalate (BHET), 2-hydroxyethyl benzoate (HEB) and dimethylterephthalate (DMT).

The time required for degrading a polyester containing material may varydepending on the polyester containing material itself (i.e., nature andorigin of the plastic product, its composition, shape etc.), the typeand amount of esterase used, as well as various process parameters(i.e., temperature, pH, additional agents, etc.). One skilled in the artmay easily adapt the process parameters to the polyester containingmaterial.

Advantageously, the degrading process is implemented at a temperaturecomprised between 20° C. and 90° C., preferably between 40° C. and 80°C., more preferably between 50° C. and 70° C., more preferably between60° C. and 70° C., even more preferably at 65° C. In another particularembodiment, the degrading process is implemented at 70° C. Moregenerally, the temperature is maintained below an inactivatingtemperature, which corresponds to the temperature at which the esteraseis inactivated and/or the recombinant microorganism does no moresynthesize the esterase. Particularly, the temperature is maintainedbelow the glass transition temperature (Tg) of the polyester in thepolyester containing material. More particularly, the process isimplemented in a continuous way, at a temperature at which the esterasecan be used several times and/or recycled.

Advantageously, the degrading process is implemented at a pH comprisedbetween 5 and 11, preferably at a pH between 6 and 9, more preferably ata pH between 6.5 and 9, even more preferably at a pH between 6.5 and 8.

In a particular embodiment, the polyester containing material may bepretreated prior to be contacted with the esterase, in order tophysically change its structure, so as to increase the surface ofcontact between the polyester and the variant of the invention.

Optionally, monomers and/or oligomers resulting from thedepolymerization may be recovered, sequentially or continuously. Asingle type of monomers and/or oligomers or several different types ofmonomers and/or oligomers may be recovered, depending on the startingpolyester containing material.

The recovered monomers and/or oligomers may be further purified, usingall suitable purifying methods and conditioned in a re-polymerizableform. Examples of purifying methods include stripping process,separation by aqueous solution, steam selective condensation, filtrationand concentration of the medium after the bioprocess, separation,distillation, vacuum evaporation, extraction, electrodialysis,adsorption, ion exchange, precipitation, crystallization, concentrationand acid addition dehydration and precipitation, nanofiltration, acidcatalyst treatment, semi continuous mode distillation or continuous modedistillation, solvent extraction, evaporative concentration, evaporativecrystallization, liquid/liquid extraction, hydrogenation, azeotropicdistillation process, adsorption, column chromatography, simple vacuumdistillation and microfiltration, combined or not.

The repolymerizable monomers and/or oligomers may then be reused forinstance to synthesize polyesters. Advantageously, polyesters of samenature are repolymerized. However, it is possible to mix the recoveredmonomers and/or oligomers with other monomers and/or oligomers, in orderfor instance to synthesize new copolymers. Alternatively, the recoveredmonomers may be used as chemical intermediates in order to produce newchemical compounds of interest.

The invention also relates to a method of surface hydrolysis or surfacefunctionalization of a polyester containing material, comprisingexposing a polyester containing material to an esterase of theinvention, or corresponding recombinant cell or extract thereof, orcomposition. The method of the invention is particularly useful forincreasing hydrophilicity, or water absorbency, of a polyester material.Such increased hydrophilicity may have particular interest in textilesproduction, electronics and biomedical applications.

It is a further object of the invention to provide a polyestercontaining material in which an esterase of the invention and/or arecombinant microorganism expressing and excreting said esterase is/areincluded. In a particular embodiment, such polyester containing materialmay be a plastic compound. It is thus an object of the invention toprovide a plastic compound containing an esterase of the inventionand/or a recombinant cell and/or a composition or extract thereof and atleast one polyester. In a preferred embodiment, the polyester is PET.

EXAMPLES Example 1—Construction, Expression and Purification ofEsterases Construction

The esterase variants have been generated using the plasmidicconstruction pET26b-LCC-His. This plasmid consists in cloning a geneencoding the esterase of SEQ ID No 1, optimized for Escherichia coliexpression between NdeI and XhoI restriction sites. Two site directedmutagenesis kits have been used according to the recommendations of thesupplier, in order to generate the esterase variants: QuikChange IISite-Directed Mutagenesis kit and QuikChange Lightning MultiSite-Directed from Agilent (Santa Clara, Calif., USA).

Expression and Purification of the Esterases

The strains Stellar™ (Clontech, Calif., USA) and E. coli One Shot® BL21DE3 (Life technologies, Carlsbad, Calif., USA) have been successivelyemployed to perform the cloning and recombinant expression in 50 mLLB-Miller medium or ZYM auto inducible medium (Studier et al.,2005—Prot. Exp. Pur. 41, 207-234). The induction in LB-Miller medium hasbeen performed at 16° C., with 0.5 mM of isopropylβ-D-1-thiogalactopyranoside (IPTG, Euromedex, Souffelweyersheim,France). The cultures have been stopped by centrifugation (8000 rpm, 20minutes at 10° C.) in an Avanti J-26 XP centrifuge (Beckman Coulter,Brea, USA). The cells have been suspended in 20 mL of Talon buffer(Tris-HCl 20 mM, NaCl 300 mM, pH 8). Cell suspension was then sonicatedduring 2 minutes with 30% of amplitude (2 sec ON and 1 sec OFF cycles)by FB 705 sonicator (Fisherbrand, Illkirch, France). Then, a step ofcentrifugation has been realized: 30 minutes at 11000 rpm, 10° C. in anEppendorf centrifuge. The soluble fraction has been collected andsubmitted to affinity chromatography. This purification step has beencompleted with Talon® Metal Affinity Resin (Clontech, Calif., USA).Protein elution has been carried out with gradient of Talon buffersupplemented with imidazole. Purified protein has been dialyzed againstTalon buffer then quantified using Bio-Rad protein assay according tomanufacturer instructions (Lifescience Bio-Rad, France) and stored at+4° C.

Example 2—Evaluation of the Activity of the Esterases

The specific activity of the esterase has been determined and comparedto the specific activity of the esterase of SEQ ID No 1.

Multiple methodologies to assess the specific activity have been used:

(1) Specific activity based upon the pNP-Butyrate hydrolysis;

(2) Specific activity based upon PET hydrolysis

(3) Specific activity based upon the degradation of a polyester undersolid form

(4) Specific activity based upon PET hydrolysis in reactors

2.1 pNP-Butyrate Hydrolysis

20 μL, of protein in solution has been combined to 175 μL, of 0.1Mpotassium phosphate buffer pH 8.0 and 50 μL, of pNP-Butyrate (40 mM in2-methyl-2-butanol). Enzymatic reaction has been performed at 30° C.under agitation, during 15 minutes and absorbance at 405 nm acquired bymicroplate spectrophotometer (Versamax, Molecular Devices, Sunnyvale,Calif., USA). Specific activity (initial velocity expressed in μmol ofreleased pNP/min/mg enzyme) has been determined in the linear part ofthe hydrolysis curve and used to compare activity of the wild typeesterase with the activity of the variants.

2.2 PET Hydrolysis

100 mg of amorphous PET were weighted and introduced in a 100 mL glassbottle. 1 mL of esterase preparation (as reference control) or variantpreparation respectively, prepared at 0.02 or 0.03 mg/mL in Talon buffer(Tris-HCl 20 mM, NaCl 0.3M, pH 8) and introduced in the glass bottle.Finally, 49 mL of 0.1 M potassium phosphate buffer pH 8 was added.

The depolymerization started by incubating each glass bottle at 65° C.and 150 rpm in a Max Q 4450 incubator (Thermo Fisher Scientific, Inc.Waltham, Mass., USA).

The initial rate of depolymerization reaction, in mg of equivalent TAgenerated/hour, was determined by samplings performed at different timeduring the first 24 hours and analyzed by Ultra High Performance LiquidChromatography (UHPLC). If necessary, samples were diluted in 0.1 Mpotassium phosphate buffer pH 8. Then, 150 μL of methanol and 6.5 μL ofHCl 6 N were added to 150 μL of sample or dilution. After mixing andfiltering on 0.45 μm syringe filter, samples were loaded on UHPLC tomonitor the liberation of terephthalic acid (TA), MHET and BHET.Chromatography system used was an Ultimate 3000 UHPLC system (ThermoFisher Scientific, Inc. Waltham, Mass., USA) including a pump module, anautosampler, a column oven thermostated at 25° C., and an UV detector at240 nm. The column used was a Discovery® HS C18 HPLC Column (150×4.6 mm,5 μm, equipped with precolumn, Supelco, Bellefonte, USA). TA, MHET andBHET were separated using a gradient of MeOH (30% to 90%) in 1 mM ofH₂SO₄ at 1 mL/min. Injection was 20 μL of sample. TA, MHET and BHET weremeasured according to standard curves prepared from commercial TA andBHET and in house synthetized MHET in the same conditions than samples.The specific activity of PET hydrolysis (mg of equivalent TA/hour/mg ofenzyme) was determined in the linear part of the hydrolysis curve.Equivalent TA corresponds to the sum of TA measured and of TA containedin measured MHET and BHET.

2.3 Degradation of a Polyester Under Solid Form

20 μL of enzyme preparation was deposited in a well created in an agarplate containing PET. Preparation of agar plates was realized bysolubilizing 500 mg of PET is solubilized in HFIP, and this medium ispoured in a 250 mL aqueous solution. After HFIP evaporation at 52° C.,the solution was mixed v/v with 0.2 M potassium phosphate buffer pH 8containing 3% agar. Around 30 mL of the mixture is used to prepare eachomnitray and stored at 4° C.

The diameters of the halos formed due to the polyester degradation bywild-type esterase and variants were measured and compared after 2 to 4hours at 60 ° C. or 65° C.

2.4 PET Hydrolysis in Reactor

A Minibio 500 bioreactors (Applikon Biotechnology B. V., Delft, TheNetherlands) was started with 5 g of amorphous PET and 100 mL of 10 mMpotassium phosphate buffer pH 8 containing 2.5 to 5 mg of esterase.Agitation was set at 250 rpm using a marine impeller. Bioreactor wasthermostated at 65° C. by immersion in an external water bath. pH wasregulated at 8 by addition of KOH at 3 M. The different parameters (pH,temperature, agitation, addition of base) were monitored thanks toBioXpert software V2.95. 500 μL of reaction medium was sampledregularly.

Amount of TA, MHET and BHET was determined by HPLC, as described inexample 2.2. Amount of EG was determined using an Aminex HPX-87K column(Bio-Rad Laboratories, Inc, Hercules, Calif., United States)thermostated at 65° C. Eluent was K₂HPO₄ 5 mM at 0.6 mL·min⁻¹. Injectionwas 20 μL. Ethylene glycol was monitored using refractometer.

The percentage of hydrolysis was calculated based on the ratio of molarconcentration at a given time (TA+MHET+BHET) versus the total amount ofTA contained in the initial sample, or based on the ratio of molarconcentration at a given time (EG+MHET+2 x BHET) versus the total amountof EG contained in the initial sample. Specific activity corresponds tospecific rate of degradation, and is calculated in mg of total liberatedequivalent TA per hour and per mg of enzyme or in mg of total equivalentEG per hour and per mg of enzyme.

Compared specific degrading activities of esterase variants of theinvention are shown in Table 1. The specific degrading activity of theesterase of SEQ ID No 1 is used as a reference and considered as 100%degrading activity. The degrading activity is measured as exposed inexample 2.2 (mg of equivalent TA/hour/mg of enzyme).

TABLE 1 Specific activity of esterase variants of the invention Variantof the invention Specific activity D63N 147% D63Q 139% F90W 112% F208I156% F208L 133% F208W 143% N211Q 112% S65T 118% S66H 113% T157E 114%T157G 116% T157N 132% T157Q 124% T176H 128% T176N 110% T176Q 144% T61M121% T61V 130% Y92G 120% Y92N 112% Y92P 177% Y92Q 155% Y92T 126% Y60M128% G53L 153% A121R 132% A121W 147% V170I 141% F208G 111% F208S 112%F208N 114% F208A 143% F208R 121% F208T 130% F208W + V170I 128% Y92P +F208L 118% Y92P + F208W 116% T176H + F208W 111% V170I + A121S 111%V170I + A121S + S223A 114% F208W + T157Q 134% F208W + T157N 137% F208W +T157S 129% F208W + S65T 189% F208W + T157E 145% F208W + D203C + S248C123% F208I + D203C + S248C 133%

Example 3—Evaluation of the Activity and Thermostability of the EsteraseVariants of the Invention

The thermostability of esterase variants of the invention has beenevaluated and compared with the thermostability of the esterase of SEQID No 1.

Differential Scanning Fluorimetry (DSF) has been used to estimatethermostability

DSF was used to evaluate the thermostability of the wild-type proteinand variants by determining their melting temperature (Tm), temperatureat which half of the protein population is unfolded. Protein sampleswere prepared at a concentration of 14 μM (0.4 mg/mL) and stored inbuffer A consisting of 20 mM Tris HCl pH 8.0, 300 mM NaCl. The SYPROorange dye 5000× stock solution in DMSO was first diluted to 250× inwater. Protein samples were loaded onto a white clear 96-well PCR plate(Bio-Rad cat #HSP9601) with each well containing a final volume of 25μl. The final concentration of protein and SYPRO Orange dye in each wellwere 5 μM (0.14 mg/ml) and 10× respectively. Loaded volumes per wellwere as follow: 15 μL of buffer A, 9 μL of the 0.4 mg/mL proteinsolution and 1 μL of the 250× Sypro Orange diluted solution. The PCRplates were then sealed with optical quality sealing tape and spun at2000 rpm for 1 min at room temperature. DSF experiments were thencarried out using a CFX96 real-time PCR system set to use the 450/490excitation and 560/580 emission filters. The samples were heated from 25to 100° C. at the rate of 1.1° C./min. A single fluorescence measurementwas taken every 0.3° C. Melting temperatures were determined byperforming a curve fit to the Boltzmann equation.

Wild-type protein and variants were then compared based on their Tmvalues. Due to high reproducibility between experiments on the sameprotein from different productions, a ΔTm of 0.8° C. was considered assignificant to compare variants. Tm values correspond to the average ofat least 2 measurements.

Compared specific degrading activities and thermostabilities of esterasevariants of the invention are shown in Table 2. The specific degradingactivity of the esterase of SEQ ID No 1 is used as a reference andconsidered as 100% degrading activity. The specific degrading activityis measured according to example 2.2 (mg of equivalent TA/hour/mg ofenzyme). The thermostability is expressed in Tm values (measuredaccording to example 3) and the gain of Tm as compared to the Tm of theesterase of SEQ ID No 1 is noted in brackets.

TABLE 2 Specific activity and Tm of the esterases of the inventionSpecific Variants of the degrading invention activity Tm of the variantof the invention F208W 143% 85.90° C. +/− 0.17° C. (+1.20° C.) Y92P 177%85.80° C. +/− 0.00° C. (+1.10° C.) T61M 121% 87.40° C. +/− 0.17° C.(+2.70° C.) Y92G 120% 87.00° C. +/− 0.00° C. (+2.30° C.) Y92P + F208W116% 86.60° C. +/− 0.17° C. (+1.90° C.) F208W + V170I 128% 85.80° C. +/−0.00° C. (+1.10° C.) F208W + D203C + 123%  94.80° C. +/− 0.00° C.(+10.10° C.) S248C F208I + D203C + 133% 90.90° C. +/− 0.00° C. (+6.20°C.) S248C

1-13. (canceled)
 14. An esterase variant which (i) has at least 75%identity to the full length amino acid sequence set forth in SEQ ID NO:1, and (ii) has at least one amino acid substitution at a positionselected from F208, T157, T176, S65, G53, A121, V170, S223, P58, A62,A64, L67, A68, N85, T86, R89, D91, P93, R96, G128, M131, G133, G134,L152, T153, P154, H156, A178, P179, H183, S206, A209, P210 or N211,wherein the positions are numbered by reference to the amino acidsequence set forth in SEQ ID NO: 1, and (iii) exhibits increasedpolyester degrading activity compared to an esterase of SEQ ID NO: 1.15. The esterase variant according to claim 14, wherein said esterasecomprises at least one amino acid substitution at a position selectedfrom F208, T157, T176, G53, A121, V170, S223, S65 or N211, wherein thepositions are numbered by reference to the amino acid sequence set forthin SEQ ID NO:
 1. 16. The esterase variant according to claim 14, whereinsaid esterase comprises at least one substitution selected from thegroup consisting of F208W/I/L/G/S/N/A/R/T, G53L, S65T, A121R/W,T157E/Q/N/G, V170I, T176H/N/Q and N211Q.
 17. The esterase variantaccording to claim 14, wherein said esterase further comprises at leastone substitution at a position selected from G59, Y60, T61, D63, S66,F90, Y92, H129, G132, W155 and V177.
 18. The esterase variant accordingto claim 17, wherein the at least one substitution is selected from thegroup consisting of Y60M/F, T61M/V, D63N/Q, S66H, F90W, andY92G/N/P/Q/T.
 19. The esterase variant according to claim 14, whereinsaid esterase comprises at least one substitution or combination ofsubstitutions selected from the group consisting ofF208W/I/L/G/S/N/A/R/T, G53L, S65T, A121R/W, T157E/Q/N/G, V170I,T176H/N/Q, N211Q, F208W+V170I, Y92P+F208L, Y92P+F208W, T176H+F208W,V170I+A121S, V170I+A121S+S223A, F208W+T157Q, F208W+T157N, F208W+T157S,F208W +S65T and F208W+T157E, wherein the positions are numbered byreference to the amino acid sequence set forth in SEQ ID NO:
 1. 20. Anucleic acid encoding an esterase variant according to claim
 14. 21. Anexpression cassette or vector comprising the nucleic acid of claim 20.22. A host cell comprising the nucleic acid of claim
 20. 23. Acomposition comprising the esterase variant as defined in claim
 14. 24.A method of producing an esterase comprising: (a) culturing the hostcell according to claim 22 under conditions suitable to express thenucleic acid encoding said esterase; and (b) recovering said esterasefrom the cell culture.
 25. A method of degrading a plastic productcontaining at least one polyester comprising (a) contacting the plasticproduct with an esterase according to claim 14 and thereby degrading theat least one polyester.
 26. The method of claim 25, further comprising(b) recovering monomers and/or oligomers resulting from the degradationof the at least one polyester.
 26. The method of claim 25, wherein theplastic product comprises at least one polyester selected frompolyethylene terephthalate (PET), polytrimethylene terephthalate (PTT),polybutylen terephthalate (PBT), polyethylene isosorbide terephthalate(PEIT), polylactic acid (PLA), polyhydroxy alkanoate (PHA), polybutylenesuccinate (PBS), polybutylene succinate adipate (PBSA), polybutyleneadipate terephthalate (PBAT), polyethylene furanoate (PEF),Polycaprolactone (PCL), poly(ethylene adipate) (PEA), polyethylenenaphthalate (PEN) and blends/mixtures of these materials.